Canonical Allele Identifier: PA2825808525
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 2114799
ClinVar RCV Id: RCV003032340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129488.1:p.Gly672Ser
CA409805671
NM_001136016.3:c.2014G>A